Skip to main content

CORRECTION article

Front. Genet., 09 June 2022
Sec. Genetics of Common and Rare Diseases
Volume 13 - 2022 | https://doi.org/10.3389/fgene.2022.931037

Corrigendum: Association of αENaC p. Ala663Thr Gene Polymorphism With Sudden Sensorineural Hearing Loss

This article is a correction to:

  1. Association of αENaC p. Ala663Thr Gene Polymorphism With Sudden Sensorineural Hearing Loss

    1. Read original article
Jialei ChenJialei Chen1Jing HeJing He1Jing LuoJing Luo2Shixun Zhong Shixun Zhong1*
  • 1Department of Otorhinolaryngology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China
  • 2Department of Pathology and Pathophysiology, Chongqing Medical University, Chongqing, China

A Corrigendum on
Association of αENaC p. Ala663Thr Gene Polymorphism With Sudden Sensorineural Hearing Loss

by Chen, J., He, J., Luo, J., Zhong, S. (2021). Front. Genet. doi:10.3389/fgene.2021.659517

In the published article, there was an error in affiliation for Jialei Chen. Instead of “2Department of Pathology and Pathophysiology, Chongqing Medical University, Chongqing, China,” it should be “1Department of Otorhinolaryngology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.”

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: sudden sensorineural hearing loss, ENaC, rs2228576, SNV, αENaC p.Ala663Thr

Citation: Chen J, He J, Luo J and Zhong S (2022) Corrigendum: Association of αENaC p. Ala663Thr Gene Polymorphism With Sudden Sensorineural Hearing Loss. Front. Genet. 13:931037. doi: 10.3389/fgene.2022.931037

Received: 28 April 2022; Accepted: 17 May 2022;
Published: 09 June 2022.

Edited and Reviewed by:

Frontiers in Genetics Editorial Office, Frontiers Media SA, Switzerland

Copyright © 2022 Chen, He, Luo and Zhong. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Shixun Zhong, zhongsx@sohu.com

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.